Zobrazeno 1 - 10
of 288
pro vyhledávání: '"M. Genuardi"'
Autor:
A. Puccini, F. Grillo, M. Fassan, S. Lonardi, M. Genuardi, R. Cannizzaro, G.M. Cavestro, F. Marmorino, V. Conca, L. Salvatore, F. Bergamo, F. Tosi, F. Morano, V. Daprà, C. Molica, D. Barana, A. Guglielmi, C. Signorelli, M. D’Amico, F. Zoratto, D. Iacono, A. Morabito, G. Martini, A. Fabbroncini, M. Duro, G. Bruera, A. Auriemma, B. Bonanni, A. Percesepe, M. Dono, L. Battistuzzi, R. Labianca, L. Boni, S. Sciallero
Publikováno v:
ESMO Gastrointestinal Oncology, Vol 3, Iss , Pp 100044- (2024)
Background: International guidelines recommend universal screening for Lynch syndrome (LS) through somatic DNA mismatch repair deficiency (dMMR) testing in all colorectal cancers (CRCs). However, LS remains largely underdiagnosed. Mainstreaming LS di
Externí odkaz:
https://doaj.org/article/350fbb2656cf4558887078dfc0237d15
Autor:
S. Sundaravel, J. Wald, R. Senker, M. Cevasco, J.H. Giri, N. Desai, J. Ortega-Legaspi, J. Pieretti, A. Owens, M. Genuardi, L. Holzhauser
Publikováno v:
The Journal of Heart and Lung Transplantation. 42:S342-S343
Autor:
J. Grewal, B. Bortner, M. Gregoski, D. Cook, A. Britt, J. Hajj, M. Rofael, M. Sheidu, M. Montovano, M. Mehta, A. Hajduczok, I. Rajapreyar, Y. Brailovski, M. Genuardi, M. Kanwar, P. Atluri, M. Lander, P. Shah, S. Hsu, A. Kilic, B. Houston, R. Tedford
Publikováno v:
The Journal of Heart and Lung Transplantation. 42:S137
Autor:
W. Bruno, B. Dalmasso, M. Barile, V. Andreotti, L. Elefanti, M. Colombino, I. Vanni, E. Allavena, F. Barbero, E. Passoni, B. Merelli, S. Pellegrini, F. Morgese, R. Danesi, V. Calò, V. Bazan, A.V. D’Elia, C. Molica, F. Gensini, E. Sala, V. Uliana, P.F. Soma, M. Genuardi, A. Ballestrero, F. Spagnolo, E. Tanda, P. Queirolo, M. Mandalà, I. Stanganelli, G. Palmieri, C. Menin, L. Pastorino, P. Ghiorzo
Publikováno v:
ESMO open. 7(4)
The incidence of cutaneous melanoma is increasing in Italy, in parallel with the implementation of gene panels. Therefore, a revision of national genetic assessment criteria for hereditary melanoma may be needed. The aim of this study was to identify
Autor:
I. Vergote, A. González-Martín, I. Ray-Coquard, P. Harter, N. Colombo, P. Pujol, D. Lorusso, M.R. Mirza, B. Brasiuniene, R. Madry, J.D. Brenton, M.G.E.M. Ausems, R. Büttner, D. Lambrechts, M. Ausems, J. Brenton, M. Abreu, S. Balboni, S. Banerjee, M. Barberis, M.P. Barretina Ginesta, J.-F. Baurain, M. Bignami, L. Bjorge, P. Blecharz, I. Bruchim, M. Capilna, N. Cerana, A. Cicchetti, D. Collins, N. Concin, M. D’Incalci, B. Davidson, T. de la Motte Rouge, P. De Iaco, F. Demirkiran, H. Denys, T. Doerk, A. Dorum, A. Ferrero, A.P. Fidalgo, M. Genuardi, L. Gladieff, R. Glasspool, C. Grimm, M. Gultekin, E. Hahnen, A. Hasenburg, A. Hegmane, V. Heinzelmann, E. Hogdall, R. Janavicius, S. Jarmalaite, R. Kalachand, R. Kaneva, S. Kilickap, R. Kocian, D. Kolencik, R. Kristeleit, A. Kryzhanivska, A. Leary, B. Lemley, M. Ligtenberg, J.A. López-Guerrero, C.J. Lord, E. Avall-Lundqvist, J. Maenpaa, S. Mahner, F. Marmé, C. Marth, I. McNeish, S. Merkelbach-Bruse, M. Mourits, N. Normanno, A. Oaknin, K. Ojamaa, C. Papdimitriou, F. Penault-Llorca, A.M. Perrone, S. Pignata, E. Pikarsky, E. Rouleau, M. Rubio, A. Sapino, B. Schmalfeldt, J. Sehouli, R. Shapira, K.D. Steffensen, V. Sukhin, J. Syrios, Z. Szallasi, C. Taskiran, M. Terzic, M. Tischkowitz, I. Toth, K. Van de Vijver, M.A. Vardar, B. Wasag, P. Wimberger, E. Witteveen
Publikováno v:
Annals of Oncology, 33, 3, pp. 276-87
Vergote, I, González-Martín, A, Ray-Coquard, I, Harter, P, Colombo, N, Pujol, P, Lorusso, D, Mirza, M R, Brasiuniene, B, Madry, R, Brenton, J D, Ausems, M G E M, Büttner, R, Lambrechts, D, European experts’ consensus group & Dahl Steffensen, K 2022, ' European experts consensus : BRCA/homologous recombination deficiency testing in first-line ovarian cancer ', Annals of Oncology, vol. 33, no. 3, pp. 276-287 . https://doi.org/10.1016/j.annonc.2021.11.013
ANNALS OF ONCOLOGY
Annals of Oncology, 33, 276-87
Vergote, I, González-Martín, A, Ray-Coquard, I, Harter, P, Colombo, N, Pujol, P, Lorusso, D, Mirza, M R, Brasiuniene, B, Madry, R, Brenton, J D, Ausems, M G E M, Büttner, R, Lambrechts, D, European experts’ consensus group & Dahl Steffensen, K 2022, ' European experts consensus : BRCA/homologous recombination deficiency testing in first-line ovarian cancer ', Annals of Oncology, vol. 33, no. 3, pp. 276-287 . https://doi.org/10.1016/j.annonc.2021.11.013
ANNALS OF ONCOLOGY
Annals of Oncology, 33, 276-87
BACKGROUND: Homologous recombination repair (HRR) enables fault-free repair of double-stranded DNA breaks. HRR deficiency is predicted to occur in around half of high-grade serous ovarian carcinomas. Ovarian cancers harbouring HRR deficiency typicall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::048b3ea84583ffb10df0f113446b4777
Autor:
L, Poliani, L, Greco, M, Barile, A Dal, Buono, P, Bianchi, G, Basso, V, Giatti, M, Genuardi, A, Malesci, L, Laghi
Publikováno v:
ESMO Open. 7:100607
Despite increasing use of next-generation sequencing (NGS), data concerning the gain in germline pathogenic variants (PVs) remain scanty, especially with respect to uncanonical ones. We aimed to verify the impact of different cancer predisposition ge
Publikováno v:
European Journal of Public Health. 31
Background Infertility is a multifactorial health issue, with males accounting for half of the cases, part of which appears to be idiopathic. Several genome-wide association studies (GWAS) have explored the role of single-nucleotide polymorphisms (SN
Autor:
John Mulvihill, J. Carda, M. Macek, M. Genuardi, Carla Easter, Daniel Fairbanks, M. Susan Lindee, V. Adam, O. Dostál, J. Sekerák, B. Křížová, Š. Pospíšilová
Publikováno v:
Genetics in Medicine. 24:S271-S272
Autor:
R Pastorino, A Tognetto, M Di Marco, E Lucci-Cordisco, M Genuardi, P Villari, M Basile, S Boccia
Publikováno v:
European Journal of Public Health. 28
Autor:
R Tricarico, M Genuardi
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Review on MUTYH (mutY homolog (E. coli)), with data on DNA, on the protein encoded, and where the gene is implicated.